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Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales

Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a prothrombotic state, but long-term effects of COVID-19 on incidence of vascular diseases are unclear. METHODS: We studied vascular diseases after COVID-19 diagnosis in population-wide anonymized linked English and...

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Autores principales: Knight, Rochelle, Walker, Venexia, Ip, Samantha, Cooper, Jennifer A., Bolton, Thomas, Keene, Spencer, Denholm, Rachel, Akbari, Ashley, Abbasizanjani, Hoda, Torabi, Fatemeh, Omigie, Efosa, Hollings, Sam, North, Teri-Louise, Toms, Renin, Jiang, Xiyun, Angelantonio, Emanuele Di, Denaxas, Spiros, Thygesen, Johan H., Tomlinson, Christopher, Bray, Ben, Smith, Craig J., Barber, Mark, Khunti, Kamlesh, Davey Smith, George, Chaturvedi, Nishi, Sudlow, Cathie, Whiteley, William N., Wood, Angela M., Sterne, Jonathan A.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484653/
https://www.ncbi.nlm.nih.gov/pubmed/36121907
http://dx.doi.org/10.1161/CIRCULATIONAHA.122.060785
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author Knight, Rochelle
Walker, Venexia
Ip, Samantha
Cooper, Jennifer A.
Bolton, Thomas
Keene, Spencer
Denholm, Rachel
Akbari, Ashley
Abbasizanjani, Hoda
Torabi, Fatemeh
Omigie, Efosa
Hollings, Sam
North, Teri-Louise
Toms, Renin
Jiang, Xiyun
Angelantonio, Emanuele Di
Denaxas, Spiros
Thygesen, Johan H.
Tomlinson, Christopher
Bray, Ben
Smith, Craig J.
Barber, Mark
Khunti, Kamlesh
Davey Smith, George
Chaturvedi, Nishi
Sudlow, Cathie
Whiteley, William N.
Wood, Angela M.
Sterne, Jonathan A.C.
author_facet Knight, Rochelle
Walker, Venexia
Ip, Samantha
Cooper, Jennifer A.
Bolton, Thomas
Keene, Spencer
Denholm, Rachel
Akbari, Ashley
Abbasizanjani, Hoda
Torabi, Fatemeh
Omigie, Efosa
Hollings, Sam
North, Teri-Louise
Toms, Renin
Jiang, Xiyun
Angelantonio, Emanuele Di
Denaxas, Spiros
Thygesen, Johan H.
Tomlinson, Christopher
Bray, Ben
Smith, Craig J.
Barber, Mark
Khunti, Kamlesh
Davey Smith, George
Chaturvedi, Nishi
Sudlow, Cathie
Whiteley, William N.
Wood, Angela M.
Sterne, Jonathan A.C.
author_sort Knight, Rochelle
collection PubMed
description Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a prothrombotic state, but long-term effects of COVID-19 on incidence of vascular diseases are unclear. METHODS: We studied vascular diseases after COVID-19 diagnosis in population-wide anonymized linked English and Welsh electronic health records from January 1 to December 7, 2020. We estimated adjusted hazard ratios comparing the incidence of arterial thromboses and venous thromboembolic events (VTEs) after diagnosis of COVID-19 with the incidence in people without a COVID-19 diagnosis. We conducted subgroup analyses by COVID-19 severity, demographic characteristics, and previous history. RESULTS: Among 48 million adults, 125 985 were hospitalized and 1 319 789 were not hospitalized within 28 days of COVID-19 diagnosis. In England, there were 260 279 first arterial thromboses and 59 421 first VTEs during 41.6 million person-years of follow-up. Adjusted hazard ratios for first arterial thrombosis after COVID-19 diagnosis compared with no COVID-19 diagnosis declined from 21.7 (95% CI, 21.0–22.4) in week 1 after COVID-19 diagnosis to 1.34 (95% CI, 1.21–1.48) during weeks 27 to 49. Adjusted hazard ratios for first VTE after COVID-19 diagnosis declined from 33.2 (95% CI, 31.3–35.2) in week 1 to 1.80 (95% CI, 1.50–2.17) during weeks 27 to 49. Adjusted hazard ratios were higher, for longer after diagnosis, after hospitalized versus nonhospitalized COVID-19, among Black or Asian versus White people, and among people without versus with a previous event. The estimated whole-population increases in risk of arterial thromboses and VTEs 49 weeks after COVID-19 diagnosis were 0.5% and 0.25%, respectively, corresponding to 7200 and 3500 additional events, respectively, after 1.4 million COVID-19 diagnoses. CONCLUSIONS: High relative incidence of vascular events soon after COVID-19 diagnosis declines more rapidly for arterial thromboses than VTEs. However, incidence remains elevated up to 49 weeks after COVID-19 diagnosis. These results support policies to prevent severe COVID-19 by means of COVID-19 vaccines, early review after discharge, risk factor control, and use of secondary preventive agents in high-risk patients.
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spelling pubmed-94846532022-09-22 Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales Knight, Rochelle Walker, Venexia Ip, Samantha Cooper, Jennifer A. Bolton, Thomas Keene, Spencer Denholm, Rachel Akbari, Ashley Abbasizanjani, Hoda Torabi, Fatemeh Omigie, Efosa Hollings, Sam North, Teri-Louise Toms, Renin Jiang, Xiyun Angelantonio, Emanuele Di Denaxas, Spiros Thygesen, Johan H. Tomlinson, Christopher Bray, Ben Smith, Craig J. Barber, Mark Khunti, Kamlesh Davey Smith, George Chaturvedi, Nishi Sudlow, Cathie Whiteley, William N. Wood, Angela M. Sterne, Jonathan A.C. Circulation Original Research Articles Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces a prothrombotic state, but long-term effects of COVID-19 on incidence of vascular diseases are unclear. METHODS: We studied vascular diseases after COVID-19 diagnosis in population-wide anonymized linked English and Welsh electronic health records from January 1 to December 7, 2020. We estimated adjusted hazard ratios comparing the incidence of arterial thromboses and venous thromboembolic events (VTEs) after diagnosis of COVID-19 with the incidence in people without a COVID-19 diagnosis. We conducted subgroup analyses by COVID-19 severity, demographic characteristics, and previous history. RESULTS: Among 48 million adults, 125 985 were hospitalized and 1 319 789 were not hospitalized within 28 days of COVID-19 diagnosis. In England, there were 260 279 first arterial thromboses and 59 421 first VTEs during 41.6 million person-years of follow-up. Adjusted hazard ratios for first arterial thrombosis after COVID-19 diagnosis compared with no COVID-19 diagnosis declined from 21.7 (95% CI, 21.0–22.4) in week 1 after COVID-19 diagnosis to 1.34 (95% CI, 1.21–1.48) during weeks 27 to 49. Adjusted hazard ratios for first VTE after COVID-19 diagnosis declined from 33.2 (95% CI, 31.3–35.2) in week 1 to 1.80 (95% CI, 1.50–2.17) during weeks 27 to 49. Adjusted hazard ratios were higher, for longer after diagnosis, after hospitalized versus nonhospitalized COVID-19, among Black or Asian versus White people, and among people without versus with a previous event. The estimated whole-population increases in risk of arterial thromboses and VTEs 49 weeks after COVID-19 diagnosis were 0.5% and 0.25%, respectively, corresponding to 7200 and 3500 additional events, respectively, after 1.4 million COVID-19 diagnoses. CONCLUSIONS: High relative incidence of vascular events soon after COVID-19 diagnosis declines more rapidly for arterial thromboses than VTEs. However, incidence remains elevated up to 49 weeks after COVID-19 diagnosis. These results support policies to prevent severe COVID-19 by means of COVID-19 vaccines, early review after discharge, risk factor control, and use of secondary preventive agents in high-risk patients. Lippincott Williams & Wilkins 2022-09-20 2022-09-20 /pmc/articles/PMC9484653/ /pubmed/36121907 http://dx.doi.org/10.1161/CIRCULATIONAHA.122.060785 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Original Research Articles
Knight, Rochelle
Walker, Venexia
Ip, Samantha
Cooper, Jennifer A.
Bolton, Thomas
Keene, Spencer
Denholm, Rachel
Akbari, Ashley
Abbasizanjani, Hoda
Torabi, Fatemeh
Omigie, Efosa
Hollings, Sam
North, Teri-Louise
Toms, Renin
Jiang, Xiyun
Angelantonio, Emanuele Di
Denaxas, Spiros
Thygesen, Johan H.
Tomlinson, Christopher
Bray, Ben
Smith, Craig J.
Barber, Mark
Khunti, Kamlesh
Davey Smith, George
Chaturvedi, Nishi
Sudlow, Cathie
Whiteley, William N.
Wood, Angela M.
Sterne, Jonathan A.C.
Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title_full Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title_fullStr Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title_full_unstemmed Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title_short Association of COVID-19 With Major Arterial and Venous Thrombotic Diseases: A Population-Wide Cohort Study of 48 Million Adults in England and Wales
title_sort association of covid-19 with major arterial and venous thrombotic diseases: a population-wide cohort study of 48 million adults in england and wales
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484653/
https://www.ncbi.nlm.nih.gov/pubmed/36121907
http://dx.doi.org/10.1161/CIRCULATIONAHA.122.060785
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